2,7-Diazabicyclo[2.2.1]heptanes: Novel Asymmetric Access and Controlled Bridge-Opening

Chemical Communications - United Kingdom
doi 10.1039/c8cc10263e
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Royal Society of Chemistry (RSC)

Related search

Synthesis of 2,7-Diazabicyclo[2.2.1]heptenes by N–O Bond Cleavage of Arylnitroso Diels–Alder 1,2-Dihydropyridine Cycloadducts

Synthesis
Organic ChemistryCatalysis
2014English

Anomalous 5-Endo-Trigreversals: General Reactions of 7-Oxabicyclo[2.2.1]heptenes and Heptanes

Canadian Journal of Chemistry
Organic ChemistryCatalysisChemistry
1984English

Asymmetric Polymerization of 2,7-Dipentyldibenzofulvene

Kobunshi Ronbunshu
Materials SciencePolymersPlasticsChemical EngineeringEnvironmental Science
2006English

Hydroxyproline-Derived Pseudoenantiomeric [2.2.1] Bicyclic Phosphines: Asymmetric Synthesis of (+)- And (−)-Pyrrolines

Journal of the American Chemical Society
BiochemistryColloidCatalysisChemistrySurface Chemistry
2014English

The Opening of the Forth Bridge

Nature
Multidisciplinary
1890English

Synthesis of Stereodefined Piperidines From Aziridines and Their Transformation Into Conformationally Constrained Amino Acids, Amino Alcohols and 2,7-Diazabicyclo[3.3.1]nonanes

Journal of Organic Chemistry
Organic Chemistry
2010English

Opening Doors for Open Access

Zeitschrift fur Anorganische und Allgemeine Chemie
Inorganic Chemistry
2019English

Opening Access by Overcoming Zeno’s Paralysis

2006English

Asymmetric Desymmetrization of Symmetric Compounds: Asymmetric Ring Opening Reactions by Chiral Catalyst.

Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
Organic Chemistry
1996English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy